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采用固相萃取和超高效液相色谱/串联质谱法检测和定量胎粪中的可卡因和苯甲酰爱康宁。

Detection and quantification of cocaine and benzoylecgonine in meconium using solid phase extraction and UPLC/MS/MS.

作者信息

Gunn Josh, Kriger Scott, Terrell Andrea R

机构信息

AIT Laboratories, Indianapolis, IN, USA.

出版信息

Methods Mol Biol. 2010;603:165-74. doi: 10.1007/978-1-60761-459-3_16.

Abstract

The simultaneous determination and quantification of cocaine and its major metabolite, benzoylecgonine, in meconium using UPLC-MS/MS is described. Ultra-performance liquid chromatography (UPLC) is an emerging analytical technique which draws upon the principles of chromatography to run separations at higher flow rates for increased speed, while simultaneously achieving superior resolution and sensitivity. Extraction of cocaine and benzoylecgonine from the homogenized meconium matrix was achieved with a preliminary protein precipitation or protein 'crash' employing cold acetonitrile, followed by a mixed mode solid phase extraction (SPE). Following elution from the SPE cartridge, eluents were dried down under nitrogen, reconstituted in 200 microL of DI water:acetonitrile (ACN) (75:25), and injected onto the UPLC/MS/MS for analysis. The increased speed and separation efficiency afforded by UPLC, allowed for the separation and subsequent quantification of both analytes in less than 2 min. Analytes were quantified using multiple reaction monitoring (MRM) and six-point calibration curves constructed in negative blood. Limits of detection for both analytes were 3 ng/g and the lower limit of quantitation (LLOQ) was 30 ng/g.

摘要

本文描述了使用超高效液相色谱-串联质谱法(UPLC-MS/MS)同时测定和定量胎粪中可卡因及其主要代谢物苯甲酰爱康宁的方法。超高效液相色谱(UPLC)是一种新兴的分析技术,它利用色谱原理,以更高的流速进行分离,从而提高速度,同时实现卓越的分离度和灵敏度。从匀浆的胎粪基质中提取可卡因和苯甲酰爱康宁,首先采用冷乙腈进行初步蛋白质沉淀或蛋白质“猝灭”,然后进行混合模式固相萃取(SPE)。从SPE柱洗脱后,洗脱液在氮气下吹干,用200微升去离子水:乙腈(ACN)(75:25)复溶,并注入UPLC/MS/MS进行分析。UPLC提供的更高速度和分离效率,使得两种分析物在不到2分钟的时间内得以分离并随后进行定量。使用多反应监测(MRM)和在阴性血液中构建的六点校准曲线对分析物进行定量。两种分析物的检测限均为3纳克/克,定量下限(LLOQ)为30纳克/克。

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